Quality and Compliance
Safe performance, our customers and quality service are of paramount importance at Albemarle. Our quality systems are robust and among the leaders in the industry. Our facilities are staffed with experienced quality control groups that operate independently from the plant operations to ensure the customer's needs and expectations are satisfied.
All of our sites maintain a quality control group that functions around the clock, 365 days per year. This group is responsible for testing and verifying that incoming raw material is within purchasing specifications, ensuring all in-process testing is in accordance with specified product and ensuring final product conformity with agreed customer specifications.
Each facility is equipped with sufficient analytical equipment to perform the required testing. A few typical pieces of analytical equipment found at our sites are below:
• HPLC autotitrators
• Mass spectrometry
• Particle size testing and polarimeters for chiral testing
Other equipment can be used or outsourced to audited and monitored third parties. Our analytical equipment is calibrated at set frequencies to ensure that our analyses are both complete and accurate.
In the pharmaceutical industry, additional quality control procedures are often required. Our site in South Haven runs under cGMPs, which bring additional quality requirements such as process and equipment validations, stability testing and documentation control. Albemarle’s quality assurance group is the guardian of the cGMP efforts and conducts activities such as batch record review and final product testing, coordination of annual product reviews, and conducting audits of raw material vendors and outside contractors, as well as coordinating customer audits.
- ISO-9000 registered, mature quality systems for over a decade
- RC/ISO-1400 environmental systems
- OSHA VPP safety systems